Clinical Insights Into Novel Immune Checkpoint Inhibitors

The success of immune checkpoint inhibitors (ICIs), notably anti-cytotoxic T lymphocyte associated antigen-4 (CTLA-4) as well as inhibitors of CTLA-4, programmed death 1 (PD-1), and programmed death ligand-1 (PD-L1), has revolutionized treatment options for solid tumors. However, the lack of respons...

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Main Authors: Jii Bum Lee, Sang-Jun Ha, Hye Ryun Kim
Format: Article
Language:English
Published: Frontiers Media S.A. 2021-05-01
Series:Frontiers in Pharmacology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fphar.2021.681320/full
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spelling doaj-2d757a8fb7a44b26a759c82b967ddf672021-05-07T12:55:13ZengFrontiers Media S.A.Frontiers in Pharmacology1663-98122021-05-011210.3389/fphar.2021.681320681320Clinical Insights Into Novel Immune Checkpoint InhibitorsJii Bum Lee0Jii Bum Lee1Sang-Jun Ha2Hye Ryun Kim3Division of Hemato-oncology, Wonju Severance Christian Hospital, Yonsei University Wonju College of Medicine, Wonju, South KoreaDivision of Medical Oncology, Department of Internal Medicine, Yonsei Cancer Center, Yonsei University College of Medicine, Seoul, South KoreaDepartment of Biochemistry, College of Life Science & Biotechnology, Yonsei University, Seoul, South KoreaDivision of Medical Oncology, Department of Internal Medicine, Yonsei Cancer Center, Yonsei University College of Medicine, Seoul, South KoreaThe success of immune checkpoint inhibitors (ICIs), notably anti-cytotoxic T lymphocyte associated antigen-4 (CTLA-4) as well as inhibitors of CTLA-4, programmed death 1 (PD-1), and programmed death ligand-1 (PD-L1), has revolutionized treatment options for solid tumors. However, the lack of response to treatment, in terms of de novo or acquired resistance, and immune related adverse events (IRAE) remain as hurdles. One mechanisms to overcome the limitations of ICIs is to target other immune checkpoints associated with tumor microenvironment. Immune checkpoints such as lymphocyte activation gene-3 (LAG-3), T cell immunoglobulin and ITIM domain (TIGIT), T cell immunoglobulin and mucin-domain containing-3 (TIM-3), V-domain immunoglobulin suppressor of T cell activation (VISTA), B7 homolog 3 protein (B7-H3), inducible T cell costimulatory (ICOS), and B and T lymphocyte attenuator (BTLA) are feasible and promising options for treating solid tumors, and clinical trials are currently under active investigation. This review aims to summarize the clinical aspects of the immune checkpoints and introduce novel agents targeting these checkpoints.https://www.frontiersin.org/articles/10.3389/fphar.2021.681320/fullimmune checkpointLAG-3TIGITTIM-3B7-H3VISTA
collection DOAJ
language English
format Article
sources DOAJ
author Jii Bum Lee
Jii Bum Lee
Sang-Jun Ha
Hye Ryun Kim
spellingShingle Jii Bum Lee
Jii Bum Lee
Sang-Jun Ha
Hye Ryun Kim
Clinical Insights Into Novel Immune Checkpoint Inhibitors
Frontiers in Pharmacology
immune checkpoint
LAG-3
TIGIT
TIM-3
B7-H3
VISTA
author_facet Jii Bum Lee
Jii Bum Lee
Sang-Jun Ha
Hye Ryun Kim
author_sort Jii Bum Lee
title Clinical Insights Into Novel Immune Checkpoint Inhibitors
title_short Clinical Insights Into Novel Immune Checkpoint Inhibitors
title_full Clinical Insights Into Novel Immune Checkpoint Inhibitors
title_fullStr Clinical Insights Into Novel Immune Checkpoint Inhibitors
title_full_unstemmed Clinical Insights Into Novel Immune Checkpoint Inhibitors
title_sort clinical insights into novel immune checkpoint inhibitors
publisher Frontiers Media S.A.
series Frontiers in Pharmacology
issn 1663-9812
publishDate 2021-05-01
description The success of immune checkpoint inhibitors (ICIs), notably anti-cytotoxic T lymphocyte associated antigen-4 (CTLA-4) as well as inhibitors of CTLA-4, programmed death 1 (PD-1), and programmed death ligand-1 (PD-L1), has revolutionized treatment options for solid tumors. However, the lack of response to treatment, in terms of de novo or acquired resistance, and immune related adverse events (IRAE) remain as hurdles. One mechanisms to overcome the limitations of ICIs is to target other immune checkpoints associated with tumor microenvironment. Immune checkpoints such as lymphocyte activation gene-3 (LAG-3), T cell immunoglobulin and ITIM domain (TIGIT), T cell immunoglobulin and mucin-domain containing-3 (TIM-3), V-domain immunoglobulin suppressor of T cell activation (VISTA), B7 homolog 3 protein (B7-H3), inducible T cell costimulatory (ICOS), and B and T lymphocyte attenuator (BTLA) are feasible and promising options for treating solid tumors, and clinical trials are currently under active investigation. This review aims to summarize the clinical aspects of the immune checkpoints and introduce novel agents targeting these checkpoints.
topic immune checkpoint
LAG-3
TIGIT
TIM-3
B7-H3
VISTA
url https://www.frontiersin.org/articles/10.3389/fphar.2021.681320/full
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